| scholarly article | Q13442814 |
| P2093 | author name string | Chiara Cianciolo Cosentino | |
| Mark de Caestecker | |||
| Alan J. Davidson | |||
| Neil A. Hukriede | |||
| Cuong Q. Diep | |||
| Lisa M. Swanhart | |||
| P2860 | cites work | Joubert Syndrome and related disorders | Q21202880 |
| Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome | Q21710711 | ||
| The Ciliopathies: An Emerging Class of Human Genetic Disorders | Q22337032 | ||
| Dissection of epistasis in oligogenic Bardet-Biedl syndrome | Q24297989 | ||
| Bardet-Biedl syndrome genes are important in retrograde intracellular trafficking and Kupffer's vesicle cilia function | Q24300539 | ||
| A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies | Q24309499 | ||
| Nephrocystin-3 is required for ciliary function in zebrafish embryos | Q24312027 | ||
| Requirement for Lim1 in head-organizer function | Q24312737 | ||
| LRRC50, a conserved ciliary protein implicated in polycystic kidney disease | Q24316336 | ||
| The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4 | Q24336477 | ||
| Genetic complexity in Joubert syndrome and related disorders | Q37018625 | ||
| The zebrafish pronephros: a model to study nephron segmentation | Q37103127 | ||
| Mechanistic insights into Bardet-Biedl syndrome, a model ciliopathy | Q37111349 | ||
| Assembly of primary cilia | Q37130367 | ||
| Building it up and taking it down: the regulation of vertebrate ciliogenesis | Q37147143 | ||
| Long-term outcomes of acute kidney injury | Q37195417 | ||
| Possible mechanisms of kidney repair | Q37265077 | ||
| Small molecule developmental screens reveal the logic and timing of vertebrate development | Q37276174 | ||
| Therapeutic and predictive targets of AKI. | Q37339377 | ||
| Inhibition of histone deacetylase activity attenuates renal fibroblast activation and interstitial fibrosis in obstructive nephropathy. | Q37417291 | ||
| Toward the identification of a "renopoietic system"? | Q37594012 | ||
| Ciliary biology: understanding the cellular and genetic basis of human ciliopathies | Q37624568 | ||
| Kidney regeneration | Q37728655 | ||
| 1001 model organisms to study cilia and flagella | Q37833124 | ||
| Uncharted waters: nephrogenesis and renal regeneration in fish and mammals | Q37845213 | ||
| Pathophysiology of ischemic acute kidney injury | Q37848648 | ||
| Developmental defects in a zebrafish model for muscular dystrophies associated with the loss of fukutin-related protein (FKRP). | Q38291016 | ||
| The nephrogenic potential of the transcription factors osr1, osr2, hnf1b, lhx1 and pax8 assessed in Xenopus animal caps | Q24338778 | ||
| Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11) | Q24546392 | ||
| The histone methyltransferase SETDB1 is recurrently amplified in melanoma and accelerates its onset | Q24625220 | ||
| Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes | Q24625476 | ||
| The many roles of histone deacetylases in development and physiology: implications for disease and therapy | Q24628821 | ||
| DHODH modulates transcriptional elongation in the neural crest and melanoma | Q24629043 | ||
| The primary cilium as a cellular signaling center: lessons from disease | Q24632942 | ||
| CC2D2A is mutated in Joubert syndrome and interacts with the ciliopathy-associated basal body protein CEP290 | Q24644138 | ||
| Mesenchymal-epithelial transition in epithelial response to injury: the role of Foxc2 | Q24645523 | ||
| Autosomal dominant polycystic kidney disease: the last 3 years | Q24656249 | ||
| Identification of a novel BBS gene (BBS12) highlights the major role of a vertebrate-specific branch of chaperonin-related proteins in Bardet-Biedl syndrome | Q24680972 | ||
| Jagged2a-notch signaling mediates cell fate choice in the zebrafish pronephric duct | Q27315061 | ||
| The nonmotile ciliopathies | Q27967648 | ||
| Genetic and physical interaction between the NPHP5 and NPHP6 gene products | Q28118065 | ||
| Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination | Q28188363 | ||
| Large scale genetics in a small vertebrate, the zebrafish | Q28286020 | ||
| Identification of a novel retinoid by small molecule screening with zebrafish embryos | Q28472496 | ||
| Genetic analysis of fin development in zebrafish identifies furin and hemicentin1 as potential novel fraser syndrome disease genes | Q28473672 | ||
| Inversin, a novel gene in the vertebrate left-right axis pathway, is partially deleted in the inv mouse | Q28504917 | ||
| Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates | Q28506652 | ||
| The ion channel polycystin-2 is required for left-right axis determination in mice | Q28508558 | ||
| Cardiac defects and renal failure in mice with targeted mutations in Pkd2 | Q28510555 | ||
| Expression and Function of the Developmental Gene Wnt-4 during Experimental Acute Renal Failure in Rats | Q28583998 | ||
| Nephric lineage specification by Pax2 and Pax8 | Q28585002 | ||
| Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene tg737, are required for assembly of cilia and flagella | Q28593253 | ||
| The primary cilium: a signalling centre during vertebrate development | Q29547197 | ||
| Inversin, the gene product mutated in nephronophthisis type II, functions as a molecular switch between Wnt signaling pathways | Q29614619 | ||
| Cilia-driven fluid flow in the zebrafish pronephros, brain and Kupffer's vesicle is required for normal organogenesis | Q29614824 | ||
| Hypomorphic mutations in syndromic encephalocele genes are associated with Bardet-Biedl syndrome | Q29615746 | ||
| Disruption of the basal body compromises proteasomal function and perturbs intracellular Wnt response | Q29617051 | ||
| Dorsomorphin inhibits BMP signals required for embryogenesis and iron metabolism | Q29617479 | ||
| Heart regeneration in zebrafish | Q29619776 | ||
| Shaping the vertebrate body plan by polarized embryonic cell movements | Q30310311 | ||
| A two-step mechanism underlies the planar polarization of regenerating sensory hair cells | Q30445500 | ||
| Neomycin-induced hair cell death and rapid regeneration in the lateral line of zebrafish (Danio rerio). | Q30473445 | ||
| Identification of an N-terminal glycogen synthase kinase 3 phosphorylation site which regulates the functional localization of polycystin-2 in vivo and in vitro | Q38510714 | ||
| Restoration of renal function in zebrafish models of ciliopathies | Q39852315 | ||
| Complex I deficiency and dopaminergic neuronal cell loss in parkin-deficient zebrafish (Danio rerio). | Q39979942 | ||
| The ADPKD genes pkd1a/b and pkd2 regulate extracellular matrix formation | Q40236123 | ||
| Antiangiogenic and vascular-targeting activity of the microtubule-destabilizing trans-resveratrol derivative 3,5,4'-trimethoxystilbene. | Q40460041 | ||
| Novel targets for Huntington's disease in an mTOR-independent autophagy pathway | Q41978909 | ||
| Intraflagellar transport proteins are essential for cilia formation and for planar cell polarity | Q41987991 | ||
| Inhibition of histone deacetylase activates side population cells in kidney and partially reverses chronic renal injury | Q42516153 | ||
| Cilia localization is essential for in vivo functions of the Joubert syndrome protein Arl13b/Scorpion | Q42644808 | ||
| A chemical genetic screen for cell cycle inhibitors in zebrafish embryos | Q42833689 | ||
| Dissection of angiogenic signaling in zebrafish using a chemical genetic approach | Q44043150 | ||
| Nephrogenesis is induced by partial nephrectomy in the elasmobranch Leucoraja erinacea | Q44449832 | ||
| Targeted expression of human MYCN selectively causes pancreatic neuroendocrine tumors in transgenic zebrafish | Q44818803 | ||
| Acute renal failure in zebrafish: a novel system to study a complex disease | Q45206207 | ||
| BRAF mutations are sufficient to promote nevi formation and cooperate with p53 in the genesis of melanoma. | Q45252786 | ||
| Ischemic acute renal failure induces the expression of a wide range of nephrogenic proteins. | Q46801058 | ||
| Proliferation capacity of the renal proximal tubule involves the bulk of differentiated epithelial cells | Q46968809 | ||
| Zebrafish curly up encodes a Pkd2 ortholog that restricts left-side-specific expression of southpaw | Q47073152 | ||
| Notch signaling controls the differentiation of transporting epithelia and multiciliated cells in the zebrafish pronephros | Q47073212 | ||
| Characterization of three novel members of the zebrafish Pax2/5/8 family: dependency of Pax5 and Pax8 expression on the Pax2.1 (noi) function | Q47073232 | ||
| A defect in a novel Nek-family kinase causes cystic kidney disease in the mouse and in zebrafish | Q47073857 | ||
| Polaris and Polycystin-2 in dorsal forerunner cells and Kupffer's vesicle are required for specification of the zebrafish left-right axis | Q47073937 | ||
| Chemical suppression of a genetic mutation in a zebrafish model of aortic coarctation | Q47074041 | ||
| A genetic screen in zebrafish identifies cilia genes as a principal cause of cystic kidney | Q47074132 | ||
| Cloning of inv, a gene that controls left/right asymmetry and kidney development. | Q48021550 | ||
| Myc-induced T cell leukemia in transgenic zebrafish | Q48392721 | ||
| Expression and function of the Delta-1/Notch-2/Hes-1 pathway during experimental acute kidney injury | Q50336844 | ||
| Light-induced rod and cone cell death and regeneration in the adult albino zebrafish (Danio rerio) retina | Q50510016 | ||
| High-throughput assay for small molecules that modulate zebrafish embryonic heart rate | Q50743158 | ||
| Kidney regeneration through nephron neogenesis in medaka | Q51829677 | ||
| Cell mosaic patterns in the native and regenerated inner retina of zebrafish: implications for retinal assembly | Q52172323 | ||
| Early development of the zebrafish pronephros and analysis of mutations affecting pronephric function | Q52182505 | ||
| A genetic screen for mutations affecting embryogenesis in zebrafish. | Q52198575 | ||
| Proximal tubular epithelial cells are generated by division of differentiated cells in the healthy kidney | Q53598069 | ||
| Primary cilia and signaling pathways in mammalian development, health and disease. | Q55443025 | ||
| Production of clones of homozygous diploid zebra fish (Brachydanio rerio) | Q59071966 | ||
| Renal cilia display length alterations following tubular injury and are present early in epithelial repair | Q62393733 | ||
| Development of newly formed nephrons in the goldfish kidney following hexachlorobutadiene-induced nephrotoxicity | Q68837244 | ||
| Infantile chronic tubulo-interstitial nephritis with cortical microcysts: variant of nephronophthisis or new disease entity? | Q69578688 | ||
| Development of New Nephrons in Adult Kidneys Following Gentamicin-Induced Nephrotoxicity | Q71982666 | ||
| A zebrafish retinoic acid receptor expressed in the regenerating caudal fin | Q72714708 | ||
| Signals from trunk paraxial mesoderm induce pronephros formation in chick intermediate mesoderm | Q73556382 | ||
| Somatic Inactivation of Pkd2 Results in Polycystic Kidney Disease | Q74502174 | ||
| High-throughput screening in academia: the Harvard experience | Q75230087 | ||
| Patterning of the avian intermediate mesoderm by lateral plate and axial tissues | Q78684881 | ||
| Transgenic zebrafish as a novel animal model to study tauopathies and other neurodegenerative disorders in vivo | Q82984434 | ||
| A genetic screen for mutations affecting embryogenesis in zebrafish | Q112778173 | ||
| Differential induction of four msx homeobox genes during fin development and regeneration in zebrafish | Q112778199 | ||
| Cancer genetics and drug discovery in the zebrafish | Q35166822 | ||
| Making a zebrafish kidney: a tale of two tubes | Q35167520 | ||
| Chemical discovery and global gene expression analysis in zebrafish | Q35190124 | ||
| Identification of adult nephron progenitors capable of kidney regeneration in zebrafish | Q35207965 | ||
| A mutation in separase causes genome instability and increased susceptibility to epithelial cancer | Q35565319 | ||
| A role for chemistry in stem cell biology | Q35824092 | ||
| Generation of a transgenic zebrafish model of Tauopathy using a novel promoter element derived from the zebrafish eno2 gene | Q36173031 | ||
| Regrow or repair: potential regenerative therapies for the kidney | Q36548118 | ||
| Adult stem cells in the repair of the injured renal tubule | Q36577069 | ||
| The changing epidemiology of acute renal failure | Q36577185 | ||
| Molecular insights into segmentation along the proximal-distal axis of the nephron. | Q36643537 | ||
| Embryonic expression of Lim-1, the mouse homolog of Xenopus Xlim-1, suggests a role in lateral mesoderm differentiation and neurogenesis | Q36721320 | ||
| Epigenetic regulation of BMP7 in the regenerative response to ischemia | Q36736738 | ||
| The subcellular localization of TRPP2 modulates its function | Q36736756 | ||
| Role of primary cilia in the pathogenesis of polycystic kidney disease | Q36788907 | ||
| lim6, a novel LIM homeobox gene in the zebrafish: Comparison of its expression pattern withlim1 | Q36877483 | ||
| Polycystin-2 immunolocalization and function in zebrafish | Q36973881 | ||
| Chemical modulation of receptor signaling inhibits regenerative angiogenesis in adult zebrafish | Q30477768 | ||
| Generation of FGF reporter transgenic zebrafish and their utility in chemical screens. | Q30479704 | ||
| Zebrafish mutations affecting cilia motility share similar cystic phenotypes and suggest a mechanism of cyst formation that differs from pkd2 morphants. | Q30482657 | ||
| A zebrafish model for Waardenburg syndrome type IV reveals diverse roles for Sox10 in the otic vesicle | Q30485384 | ||
| Convergent extension movements and ciliary function are mediated by ofd1, a zebrafish orthologue of the human oral-facial-digital type 1 syndrome gene | Q30485917 | ||
| Characterization of mesonephric development and regeneration using transgenic zebrafish | Q30497359 | ||
| Intrarenal cells, not bone marrow-derived cells, are the major source for regeneration in postischemic kidney | Q33218591 | ||
| The cdx genes and retinoic acid control the positioning and segmentation of the zebrafish pronephros | Q33303450 | ||
| Automated, quantitative screening assay for antiangiogenic compounds using transgenic zebrafish | Q33308472 | ||
| Zebrafish chemical screening reveals an inhibitor of Dusp6 that expands cardiac cell lineages | Q33478364 | ||
| Chemical modifier screen identifies HDAC inhibitors as suppressors of PKD models | Q33564416 | ||
| Nephronophthisis: disease mechanisms of a ciliopathy | Q33594278 | ||
| Zebrafish heart regeneration occurs by cardiomyocyte dedifferentiation and proliferation | Q33757338 | ||
| Automated image-based phenotypic analysis in zebrafish embryos | Q33818305 | ||
| Inhibition of histone deacetylase expands the renal progenitor cell population | Q33834281 | ||
| Kidney morphogenesis: cellular and molecular regulation | Q33855366 | ||
| Restoration of tubular epithelial cells during repair of the postischemic kidney occurs independently of bone marrow-derived stem cells | Q33865856 | ||
| A large-scale insertional mutagenesis screen in zebrafish | Q33878395 | ||
| Functional analyses of variants reveal a significant role for dominant negative and common alleles in oligogenic Bardet-Biedl syndrome | Q33934745 | ||
| Frequency of gamma-Ray Induced Specific Locus and Recessive Lethal Mutations in Mature Germ Cells of the Zebrafish, BRACHYDANIO RERIO. | Q33949041 | ||
| Induction of Mutations by gamma-Rays in Pregonial Germ Cells of Zebrafish Embryos | Q33949046 | ||
| Genetic interaction between Bardet-Biedl syndrome genes and implications for limb patterning | Q33979104 | ||
| Localization of proliferating cell nuclear antigen, vimentin, c-Fos, and clusterin in the postischemic kidney. Evidence for a heterogenous genetic response among nephron segments, and a large pool of mitotically active and dedifferentiated cells. | Q34146136 | ||
| The cell biology of polycystic kidney disease | Q34149966 | ||
| Differential induction of four msx homeobox genes during fin development and regeneration in zebrafish | Q34311992 | ||
| Kidney development and disease in the zebrafish | Q34383970 | ||
| A fish model of renal regeneration and development | Q34388142 | ||
| Primary contribution to zebrafish heart regeneration by gata4(+) cardiomyocytes. | Q34618217 | ||
| Nephronophthisis-associated ciliopathies | Q34629900 | ||
| Intrinsic epithelial cells repair the kidney after injury | Q34765013 | ||
| The pronephros. | Q34919565 | ||
| Dedifferentiation and proliferation of surviving epithelial cells in acute renal failure | Q35133244 | ||
| Intravenous Microinjections of Zebrafish Larvae to Study Acute Kidney Injury | Q35164175 | ||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | animal model | Q264024 |
| Danio rerio | Q169444 | ||
| P304 | page(s) | 141-156 | |
| P577 | publication date | 2011-06-01 | |
| P13046 | publication type of scholarly work | review article | Q7318358 |
| P1433 | published in | Birth Defects Research Part C: Embryo Today Reviews | Q15757886 |
| P1476 | title | Zebrafish kidney development: basic science to translational research | |
| Zebrafish kidney development: Basic science to translational research | |||
| P478 | volume | 93 |
| Q48126211 | A nonsense mutation in CEP55 defines a new locus for a Meckel-like syndrome, an autosomal recessive lethal fetal ciliopathy. |
| Q35694396 | Analysis of nephron composition and function in the adult zebrafish kidney |
| Q36580550 | Apical Targeting and Endocytosis of the Sialomucin Endolyn are Essential for Establishment of Zebrafish Pronephric Kidney Function |
| Q84565605 | Assessing cardio‐renal function in zebrafish larvae |
| Q35673700 | Atlas of Cellular Dynamics during Zebrafish Adult Kidney Regeneration |
| Q34564022 | Centrosomes in the zebrafish (Danio rerio): a review including the related basal body |
| Q38198032 | Congenital and Acute Kidney Disease: Translational Research Insights from Zebrafish Chemical Genetics |
| Q36780455 | Current insights into renal ciliopathies: what can genetics teach us? |
| Q36810715 | Delayed treatment with PTBA analogs reduces postinjury renal fibrosis after kidney injury |
| Q52607044 | Drug Discovery to Halt the Progression of Acute Kidney Injury to Chronic Kidney Disease: A Case for Phenotypic Drug Discovery in Acute Kidney Injury |
| Q99584589 | Exploring Key Challenges of Understanding the Pathogenesis of Kidney Disease in Bardet-Biedl Syndrome |
| Q34155624 | Fish is Fish: the use of experimental model species to reveal causes of skeletal diversity in evolution and disease |
| Q98937067 | Fishing for protective compounds |
| Q36456375 | Galanin regulates blood glucose level in the zebrafish: a morphological and functional study |
| Q36068284 | Hooked! Modeling human disease in zebrafish |
| Q26765261 | Insights into kidney stem cell development and regeneration using zebrafish |
| Q59792055 | Investigating the RAS can be a fishy business: interdisciplinary opportunities using Zebrafish |
| Q38794766 | Ion transport in the zebrafish kidney from a human disease angle: possibilities, considerations, and future perspectives. |
| Q27694725 | Kidney organogenesis in the zebrafish: insights into vertebrate nephrogenesis and regeneration |
| Q36906009 | Little fish, big catch: zebrafish as a model for kidney disease |
| Q28312156 | Making a Tubule the Noncanonical Way |
| Q64082612 | Moderate Nucleoporin 133 deficiency leads to glomerular damage in zebrafish |
| Q37582455 | New model systems to illuminate thyroid organogenesis. Part I: an update on the zebrafish toolbox |
| Q36838519 | OCRL1 modulates cilia length in renal epithelial cells. |
| Q28067647 | Renal progenitors: Roles in kidney disease and regeneration |
| Q33635081 | Roles of Iroquois Transcription Factors in Kidney Development. |
| Q42778078 | The transcriptional response of skin to fluorescent light exposure in viviparous (Xiphophorus) and oviparous (Danio, Oryzias) fishes |
| Q47226520 | Translating Knowledge Into Therapy for Acute Kidney Injury |
| Q34206971 | Using zebrafish to study podocyte genesis during kidney development and regeneration |
| Q30528767 | Wtip and Vangl2 are required for mitotic spindle orientation and cloaca morphogenesis |
| Q37190836 | Wtip is required for proepicardial organ specification and cardiac left/right asymmetry in zebrafish |
| Q55689509 | Zebrafish as a Model for Drug Screening in Genetic Kidney Diseases. |
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